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C102202

Sigma-Aldrich

Cyclohexanone oxime

97%

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About This Item

Fórmula lineal:
C6H10(=NOH)
Número de CAS:
100-64-1
Peso molecular:
113.16
Beilstein/REAXYS Number:
1616769
EC Number:
202-874-0
MDL number:
MFCD00001660
UNSPSC Code:
12352100
PubChem Substance ID:
24892305
NACRES:
NA.22

assay

97%

form

crystals

bp

206-210 °C (lit.)

mp

86-89 °C (lit.)

SMILES string

O\N=C1/CCCCC1

InChI

1S/C6H11NO/c8-7-6-4-2-1-3-5-6/h8H,1-5H2

InChI key

VEZUQRBDRNJBJY-UHFFFAOYSA-N

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pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Raphaël Turgis et al.
ChemSusChem, 3(12), 1403-1408 (2010-12-01)
Brønsted-acidic ionic liquids that bear a sulfonic acid group, known as Forbes acids, show a good catalytic activity for the Beckmann rearrangement, used to prepare ε-caprolactam, which is a precursor of Nylon 6. The activity essentially stems from the acidity of
D Parmar et al.
Drug metabolism and disposition: the biological fate of chemicals, 19(6), 1101-1107 (1991-11-01)
Cyclohexanone oxime (CHOX), an intermediate used in the synthesis of Polycaprolactam/Nylon, was found to be rapidly absorbed and cleared from the body within 24 hours after a single oral administration of 1, 10 and 30 mg/kg of [14C]-CHOX to the
M J Prival
Mutation research, 497(1-2), 1-9 (2001-08-30)
The basis for the observed mutagenicity of cyclohexanone oxime in the presence of hamster liver S9 in Salmonella typhimurium strain TA1535, but not in TA100, was explored. While the chemical had no effect on the appearance of the background lawn
Wen-Cui Li et al.
Journal of the American Chemical Society, 127(36), 12595-12600 (2005-09-08)
In this study, we present a synthetic pathway for the fabrication of self-supporting zeolite monoliths consisting of crystallized nanoparticles. A resorcinol-formaldehyde-based organic aerogel is used as a template, and silicalite-1 is used as the zeolite example. The silicalite-1 monoliths obtained
S C Gad et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 5(1), 128-136 (1985-02-01)
Dermal exposure of rabbits to cyclohexanone oxime (CHO) for 24 hr at 0, 0.8, 2, and 5 g/kg caused dose-related reticulocytosis on the day after dosing as well as a decrease in hemoglobin in the 5-g/kg females 7 days postdosing.
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